A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv55n145



Internal ID22813071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89630429..89635934hg38UCSC Ensembl
chr1:90095988..90101493hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg385506
hg195506
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3118215, nsv3115440, nsv3118216
Samplessample81, sample300, sample296
Known GenesFLJ27354, LRRC8C
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv55n145
Frequency
Sample Size467
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer